Microstructurally controlled mullite ceramics produced from monophasic and diphasic sol-derived pastes using extrusion
Source abstract
Abstract
Mullite ceramics with controlled microstructure in terms of grain size/shape, pore and glassy phase content were produced from sol-derived pastes using extrusion. Particular attention has been given to the development of a continuous process which is suitable for the preparation of high-solids-loading mullite pastes from two different starting mullite precursors, namely, diphasic and molecular mixed mullite sols. A combined processing technique comprising vacuum filtering and pressure filtration was introduced in order to obtain extrudable mullite pastes from low solids-loading colloidal sols. It is shown that glassy phase free stoichiometric 3:2 mullite (3Al2O3·2SiO2) with fine (0.94 μm) equiaxed grain microstructure is achievable from monophasic precursors after pressureless sintering at 1400°C for 3 h using the developed technique which can control both the sol-derived paste microstructure and process parameters. It is also found that the room and high temperature (1300°C) flexural strength and toughness of extruded mullites are mainly controlled by the grain size, the presence and location of glassy phase, nano-inclusions and pores at the grain boundaries. Pressureless sintered mullite derived from the monophasic sol-derived pastes provides flexural strength values of 345 and 277 M Pa for room temperature and 1300°C, respectively.
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Research context
OpenAlex topics: Advanced ceramic materials synthesis · Microwave Dielectric Ceramics Synthesis · Synthesis and properties of polymers
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References (19)
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1. S. Somiya, R. F. Davis and J. A. Pask (eds.), “Ceramics Transactions” Vol. 6; Mullite and Mullite Matrix Composites. (American Ceramic Society, Westerville, OH, 1990).
2. S. Kanzaki, H. Tabata, T. Kumazawa and S. Ohta, J. Amer. Ceram. Soc. 68 (1985) C-6.10.1111/j.1151-2916.1985.tb15252.x ↗
3. H. Schneider, H. Okada and J. A. Pask (eds.), “Mullite and Mullite Ceramics” (John Wiley & Sons, Chichester, 1994).
4. B. E. Yoldas, J. Mater. Sci. 27 (1992) 6667.10.1007/BF01165952 ↗
5. W.-C. Wei and J. W. Halloran, J. Amer. Ceram. Soc. 71 (1988) 581.10.1111/j.1151-2916.1988.tb05923.x ↗
6. D. W. Hoffman, R. Roy and S. Komarneni, ibid. 67 (1984) 468.10.1111/j.1151-2916.1984.tb19636.x ↗
7. C. Kaya, P. A. Trusty and C. B. Ponton, Brit. Ceram. Trans. 97 (1998) 48.
8. J. Huling and G. L. Messing, J. Non-Cryst. Solids. 147/148 (1992) 213.10.1016/S0022-3093(05)80620-9 ↗
9. D.X. Li and W. Thomson, J. Amer. Ceram. Soc. 73 (1990) 964.10.1111/j.1151-2916.1990.tb05144.x ↗
10. Y. Wang and W. J. Thomson, J. Mater. Res. 10 (1995) 912.10.1557/JMR.1995.0912 ↗
11. G. R. Antis, P. Chantikul, B. R. Lawn and D. B. Marshall, J. Amer. Ceram. Soc. 64 (1985) 539.
12. M. I. Mendelson, ibid. 52 (1969) 443.10.1111/j.1151-2916.1969.tb11975.x ↗
13. C. Kaya, PhD thesis, The University of Birmingham, UK, June 1999.
14. C. Kaya, F.Kaya and A. R. Boccaccini, Adv. Engineering Materials 4 (2002) 21.10.1002/1527-2648(20020212)4:1/2<21::AID-ADEM21>3.0.CO;2-O ↗
15. N. Tamari, T. Tanaka, I. Kondoh and S. Kose, J. Ceram. Soc. Jpn. 99 (1991) 89.10.2109/jcersj.99.89 ↗
16. R. Ruh, K. S. Mazdiyasni and M. G. Mendiratta, J. Amer. Ceram. Soc. 71 (1986) 503.10.1111/j.1151-2916.1988.tb05902.x ↗
17. K. Rundgren, P. Elfving, H. Tabata and S. Kanzaki, Ceram. Trans. 6 (1990) 553.
18. C. Nischik, M. M. Seibold, N. A. Travitzky and N. Claussen, J. Amer. Ceram. Soc. 74 (1991) 2464.10.1111/j.1151-2916.1991.tb06786.x ↗
19. Y. Yamade, Y. Kawaguchi, N. Takeda and T. Kishi, J. Ceram. Soc. Jpn. D 14 (1990) 2.